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Study identifier: NCT06836986 Synced from ClinicalTrials.gov · July 29, 2026
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COMPARISON BETWEEN EFFICACY OF NOREPINEPHRINE AND PHENYLEPHRINE BOLUSES for PREVENTION OF SPINAL ANAESTHESIA INDUCED HYPOTENSION IN OBSTETRICAL PATIENTS UNDERGOING EMERGENCY CESAREAN SECTION-A Double Blind Randomized Controlled Trial

Condition: Spinal Anesthesia Induced Hypotension  ·  Sponsor: Dow University of Health Sciences

PhaseNA
Planned participants124
Who can joinFemale, 18 Years to 40 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to learn if norepinephrine is more effective than phenylephrine for prevention of spinal anesthesia induced hypotension. The main questions it aims to answer are: Does norepinephrine lower the incidence of spinal anesthesia induced hypotension in emergency obstetrical patients? We will compare effectiveness of norepinephrine and phenylephrine for the prevention of spinal anesthesia induced hypotension. Participants will: Be administered prophylactic boluses of both drugs right after spinal anesthesia induction and maternal hemodynamic parameters and neonatal APGAR scores will be recorded

This description comes directly from the study's public registry record.

Talk to the study team

Rabia Kamal, MBBS  ·  923342239607  ·  rabiakamal.ae@gmail.com

Arsalan Jamil, FCPS  ·  923341226693  ·  22arsalan@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Dr Ruth km pfau civil hospital karachi Dow University of health sciences, department of anesthesiologyKarachi, Sindh, PakistanRecruiting

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Source record: clinicaltrials.gov/study/NCT06836986